scholarly journals Estimated variability of below-cloud aerosol removal by rainfall for observed aerosol size distributions

2003 ◽  
Vol 3 (1) ◽  
pp. 131-143 ◽  
Author(s):  
C. Andronache
Keyword(s):  
Size Distribution ◽  
Field Experiments ◽  
Numerical Models ◽  
Aerosol Particles ◽  
Rainfall Rate ◽  
Aerosol Size Distribution ◽  
Size Distributions ◽  
Aerosol Mass Concentration ◽  
Raindrop Size Distribution ◽  
Cloud Scavenging

Abstract. Below-cloud scavenging (BCS) coefficients of aerosols by rainfall are estimated for reported aerosol size distributions measured during field experiments in various environments. The method employed is based on explicit calculations of the efficiency of collision between a raindrop and aerosol particles. Such BCS coefficients can be used in numerical models that describe: 1) the detailed evolution of aerosol size distribution and, 2) the evolution of total aerosol mass concentration. The effects of raindrop size distribution and aerosol size distribution variability on BCS coefficients are illustrated using observed data. Results show that BCS coefficient increases with rainfall rate and has a significant dependence on aerosol size distribution parameters. Thus, BCS is important for very small particles (with diameters less than 0.01 μm) and for coarse particles (with diameters larger than 2 µm). For rainfall rate R ~ 1 mm hr-1, the 0.5-folding time of these particles is of the order of one hour. It is shown that BCS is negligible for aerosol particles in the range [0.1-1] µm if compared with in-cloud scavenging rates for low and moderate rainfall rates ( R ~ 0.1-10 mm hr-1). The results indicate that a boundary layer aerosol size distribution with coarse mode is drastically affected very shortly after rain starts (in a fraction of one hour) and consequently, the below-cloud aerosol size distribution becomes dominated by particles in the accumulation mode.

scholarly journals Estimated variability of below-cloud aerosol removal by rainfall for observed aerosol size distributions

2002 ◽  
Vol 2 (6) ◽  
pp. 2095-2131 ◽  
Author(s):  
C. Andronache
Keyword(s):  
Size Distribution ◽  
Field Experiments ◽  
Aerosol Particles ◽  
Rainfall Rate ◽  
Aerosol Size Distribution ◽  
Size Distributions ◽  
Coarse Particles ◽  
Distribution Parameters ◽  
Cloud Scavenging ◽  
Scavenging Rates

Abstract. Below-cloud scavenging (BCS) coefficients of aerosols by rainfall are estimated for reported aerosol size distributions measured during field experiments in various environments. The method employed is based on explicit calculations of the efficiency of collision between a raindrop and aerosol particles. Results show that BCS coefficient increases with rainfall rate and has a significant dependence on aerosol size distribution parameters. Thus, BCS is important for very small particles (with diameters less than 0.01 µm) and for coarse particles (with diameters larger than 2 µm). For rainfall rate R ~ 1 mm hr -1, the 0.5-folding time of these particles is of the order of one hour. It is shown that BCS is negligible for aerosol particles in the range [0.1-1] µm if compared with in-cloud scavenging rates for low and moderate rainfall rates (R ~ 0.1-10 mm hr -1). The results indicate that a boundary layer aerosol size distribution with coarse mode is drastically affected very shortly after rain starts (in a fraction of one hour) and consequently, the below-cloud aerosol size distribution becomes dominated by particles in the accumulation mode.

scholarly journals On the Shape–Slope Relation of Drop Size Distributions in Convective Rain

2005 ◽  
Vol 44 (7) ◽  
pp. 1146-1151 ◽  
Author(s):  
Axel Seifert
Keyword(s):  
Size Distribution ◽  
Gamma Distribution ◽  
Drop Size ◽  
Empirical Relation ◽  
Size Distributions ◽  
Shape Parameters ◽  
Raindrop Size Distribution ◽  
Raindrop Size ◽  
Drop Size Distributions ◽  
Good Agreement

Abstract The relation between the slope and shape parameters of the raindrop size distribution parameterized by a gamma distribution is examined. The comparison of results of a simple rain shaft model with an empirical relation based on disdrometer measurements at the surface shows very good agreement, but a more detailed discussion reveals some difficulties—for example, deviations from the gamma shape and the overestimation of collisional breakup.

Determination of atmospheric aerosol particle size distribution and visibility using a mobile laboratory

1982 ◽  
Vol 60 (8) ◽  
pp. 1101-1107
Author(s):  
C. V. Mathai ◽  
A. W. Harrison
Keyword(s):  
Particle Size ◽  
Particle Size Distribution ◽  
Size Distribution ◽  
Atmospheric Aerosols ◽  
Suspended Particle ◽  
Aerosol Size Distribution ◽  
Size Distributions ◽  
Mobile Laboratory ◽  
Mean Values ◽  
The City

As part of an ongoing general research program on the effects of atmospheric aerosols on visibility and its dependence on aerosol size distributions in Calgary, this paper presents the results of a comparative study of particle size distribution and visibility in residential (NW) and industrial (SE) sections of the city using a mobile laboratory. The study was conducted in the period October–December, 1979. An active scattering aerosol spectrometer measured the size distributions and the corresponding visibilities were deduced from scattering coefficients measured with an integrating nephelometer.The results of this transit study show significantly higher suspended particle concentrations and reduced visibilities in the SE than in the NW. The mean values of the visibilities are 44 and 97 km for the SE and the NW respectively. The exponent of R (particle radius) in the power law aerosol size distribution has a mean value of −3.36 ± 0.24 in the SE compared with the corresponding value of −3.89 ± 0.39 for the NW. These results arc in good agreement with the observations of Alberta Environment; however, they are in contradiction with a recent report published by the City of Calgary.

scholarly journals An investigation of processes controlling the evolution of the boundary layer aerosol size distribution properties at the Swedish background station Aspvreten

2004 ◽  
Vol 4 (4) ◽  
pp. 4507-4543 ◽  
Author(s):  
P. Tunved ◽  
J. Ström ◽  
H.-C. Hansson
Keyword(s):  
Size Distribution ◽  
Wet Deposition ◽  
Source Area ◽  
Aerosol Size Distribution ◽  
Back Trajectory ◽  
Main Process ◽  
Size Distributions ◽  
Back Trajectory Analysis ◽  
The One ◽  
Precipitating Clouds

Abstract. Aerosol size distributions have been measured at the Swedish background station Aspvreten (58.8° N, 17.4° E). Different states of the aerosol were determined using a novel application of cluster analysis. The analysis resulted in eight different clusters capturing the different stages of the aerosol lifecycle. The aerosol was interpreted as belonging to fresh, intermediate and aged type of size distribution and different magnitudes thereof. With aid of back trajectory analysis we present statistics concerning the relation of source area and different meteorological parameters using a non-lagrangian approach. Source area is argued to be important although not sufficient to describe the observed aerosol properties. Especially processing by clouds and precipitation is shown to be crucial for the evolution of the aerosol size distribution. As much as 60% of the observed size distributions present features likely related to cloud processes or wet deposition. The lifetime properties of different sized aerosols are discussed by means of measured variability. Processing by non-precipitating clouds most obviously affect aerosols in the size range 100 nm and larger. This indicates an approximate limit for activation in clouds to 100 nm in this type of environment. The aerosol lifecycle is discussed. Size distributions bearing signs of recent new particle formation (~30% of the observed size distributions) represent the first stage in the lifecycle. Aging may proceed in two directions: either growth by condensation and coagulation or processing by non-precipitating clouds. In both cases mass is accumulated. Wet removal is the main process capable of removing aerosol mass. Wet deposition is argued to be an important mechanism in reaching a state where nucleation may occur (i.e. sufficiently low aerosol surface area) in environments similar to the one studied.

scholarly journals Quantifying aerosol size distributions and their temporal variability in the Southern Great Plains, USA

2019 ◽  
Vol 19 (18) ◽  
pp. 11985-12006 ◽  
Author(s):  
Peter J. Marinescu ◽  
Ezra J. T. Levin ◽  
Don Collins ◽  
Sonia M. Kreidenweis ◽  
Susan C. van den Heever
Keyword(s):  
Size Distribution ◽  
Great Plains ◽  
Diurnal Cycle ◽  
Particle Formation ◽  
Aerosol Size Distribution ◽  
Size Distributions ◽  
New Particle Formation ◽  
Scanning Mobility Particle Sizer ◽  
Southern Great Plains ◽  
Particle Sizer

Abstract. A quality-controlled, 5-year dataset of aerosol number size distributions (particles with diameters (Dp) from 7 nm through 14 µm) was developed using observations from a scanning mobility particle sizer, aerodynamic particle sizer, and a condensation particle counter at the Department of Energy's Southern Great Plains (SGP) site. This dataset was used for two purposes. First, typical characteristics of the aerosol size distribution (number, surface area, and volume) were calculated for the SGP site, both for the entire dataset and on a seasonal basis, and size distribution lognormal fit parameters are provided. While the median size distributions generally had similar shapes (four lognormal modes) in all the seasons, there were some significant differences between seasons. These differences were most significant in the smallest particles (Dp<30 nm) and largest particles (Dp>800 nm). Second, power spectral analysis was conducted on this long-term dataset to determine key temporal cycles of total aerosol concentrations, as well as aerosol concentrations in specified size ranges. The strongest cyclic signal was associated with a diurnal cycle in total aerosol number concentrations that was driven by the number concentrations of the smallest particles (Dp<30 nm). This diurnal cycle in the smallest particles occurred in all seasons in ∼50 % of the observations, suggesting a persistent influence of new particle formation events on the number concentrations observed at the SGP site. This finding is in contrast with earlier studies that suggest new particle formation is observed primarily in the springtime at this site. The timing of peak concentrations associated with this diurnal cycle was shifted by several hours depending on the season, which was consistent with seasonal differences in insolation and boundary layer processes. Significant diurnal cycles in number concentrations were also found for particles with Dp between 140 and 800 nm, with peak concentrations occurring in the overnight hours, which were primarily associated with both nitrate and organic aerosol cycles. Weaker cyclic signals were observed for longer timescales (days to weeks) and are hypothesized to be related to the timescales of synoptic weather variability. The strongest periodic signals (3.5–5 and 7 d cycles) for these longer timescales varied depending on the season, with no cyclic signals and the lowest variability in the summer.

scholarly journals Application of absolute principal component analysis to size distribution data: identification of particle origins

2007 ◽  
Vol 7 (3) ◽  
pp. 887-897 ◽  
Author(s):  
T. W. Chan ◽  
M. Mozurkewich
Keyword(s):  
Principal Component Analysis ◽  
Size Distribution ◽  
Aerosol Particles ◽  
Principal Component ◽  
Component Analysis ◽  
Trace Gas ◽  
Rural Site ◽  
Aerosol Size Distribution ◽  
Urban Site ◽  
Distribution Data

Abstract. Absolute principal component analysis can be applied, with suitable modifications, to atmospheric aerosol size distribution measurements. This method quickly and conveniently reduces the dimensionality of a data set. The resulting representation of the data is much simpler, but preserves virtually all the information present in the original measurements. Here we demonstrate how to combine the simplified size distribution data with trace gas measurements and meteorological data to determine the origins of the measured particulate matter using absolute principal component analysis. We have applied the analysis to four different sets of field measurements that were conducted at three sites in southern Ontario. Several common factors were observed at all the sites; these were identified as photochemically produced secondary aerosol particles, regional pollutants (including accumulation mode aerosol particles), and trace gas variations associated with boundary layer dynamics. Each site also exhibited a factor associated specifically with that site: local industrial emissions in Hamilton (urban site), processed nucleation mode particles at Simcoe (polluted rural site), and transported fine particles at Egbert (downwind from Toronto).

scholarly journals On the Quantitative Low-Level Aerosol Measurements Using Ceilometer-Type Lidar

2009 ◽  
Vol 26 (11) ◽  
pp. 2340-2352 ◽  
Author(s):  
Anu-Maija Sundström ◽  
Timo Nousiainen ◽  
Tuukka Petäjä
Keyword(s):  
Size Distribution ◽  
Theoretical Calculations ◽  
Measurement Instrument ◽  
Aerosol Size Distribution ◽  
Lidar Measurement ◽  
Size Distributions ◽  
Absolute Accuracy ◽  
Particle Composition ◽  
Aerosol Measurement

Abstract The objective of this work is to investigate whether a commercial ceilometer-type lidar can be used as a quantitative aerosol measurement instrument. To this end, lidar backscattering measurements are compared with exact theoretical calculations of backscattering, which are based on in situ–measured size distributions and account for uncertainties in particle composition and shape. The results show that the differences between simulated and measured backscattering remain nearly constant and within the uncertainties involved. The differences are most plausibly explained by an error in the overlap function of the lidar and/or errors in the calibration of either the lidar or the in situ instruments used to measure the aerosol size distribution. Occasionally, large differences occur that are obviously connected to the unrepresentativeness of the in situ and lidar measurement volumes because of insufficient atmospheric mixing. The results imply that the absolute accuracy of the instrument investigated might be sufficient for quantitative aerosol measurements in some applications. A fix for the overlap function, however, would be desirable.

scholarly journals Determination of Fitted Size Distribution for Atmospheric Aerosols

2017 ◽  
Vol 14 (2) ◽  
Author(s):  
Kaitlin DuPaul ◽  
Adam Whitten
Keyword(s):  
Particle Swarm Optimization ◽  
Size Distribution ◽  
Atmospheric Aerosols ◽  
Particle Swarm ◽  
Bimodal Distribution ◽  
Aerosol Size Distribution ◽  
Size Distributions ◽  
Swarm Optimization ◽  
Large Variability ◽  
Lognormal Distributions

A synthetic set of aerosol optical depths (AODs) generated from a standard set of aerosol size distributions was analyzed by a parameter based particle swarm optimization (PBPSO) routine in order to test the reproducibility of the results. Junge and lognormal size distributions were consistently reproduced. Gamma and bimodal distributions showed large variability in solutions. values were used to determine the best subset of possible solutions allowing quantification of parameters with uncertainties when using PBPSO. AODs measured by a sun photometer on a clear day (20160413) and a foggy day (20160508) were then processed by the PBPSO program for both bimodal and lognormal distributions. Results showed that in general the foggy day has smaller values indicating that the PBPSO algorithm is better able to match AODs when there is a larger aerosol load in the atmosphere. The bimodal distribution from the clear day best describes the aerosol size distribution since the values are lower. The lognormal distribution best describes the aerosol size distribution on the foggy day (20160508). KEYWORDS: Atmospheric Aerosols; Size Distributions; Junge; Bimodal; Gamma; Lognormal; Particle Swarm Optimization; Inverse Problem; Aerosol Optical Depth

scholarly journals Impact of aerosol composition on cloud condensation nuclei activity

2012 ◽  
Vol 12 (8) ◽  
pp. 3783-3790 ◽  
Author(s):  
Q. Zhang ◽  
J. Meng ◽  
J. Quan ◽  
Y. Gao ◽  
D. Zhao ◽  
...  
Keyword(s):  
Size Distribution ◽  
Field Experiments ◽  
Cloud Condensation Nuclei ◽  
Diffusion Chamber ◽  
Aerosol Size Distribution ◽  
Condensation Nuclei ◽  
Aerosol Composition ◽  
Rate Of Increase ◽  
The Impact ◽  
Ccn Activity

Abstract. The impact of aerosol composition on cloud condensation nuclei (CCN) activity were analyzed in this study based on field experiments carried out at downtown Tianjin, China in September 2010. In the experiments, the CCN measurements were performed at supersaturation (SS) of 0.1%, 0.2% and 0.4% using a thermal-gradient diffusion chamber (DMT CCNC), whereas the aerosol size distribution and composition were simultaneously measured with a TSI SMPS and an Aerodyne Aerosol Mass Spectrometer (AMS), respectively. The results show that the influence of aerosol composition on CCN activity is notable under low SS (0.1%), and their influence decreased with increasing SS. For example, under SS of 0.1%, the CCN activity increases from 4.5±2.6% to 12.8±6.1% when organics fraction decrease from 30–40% to 10–20%. The rate of increase reached up to 184%. While under SS of 0.4%, the CCN activity increases only from 35.7±19.0% to 46.5±12.3% correspondingly. The calculated NCCN based on the size-resolved activation ratio and aerosol number size distribution correlated well with observed NCCN at high SS (0.4%), but this consistence decreased with the falling of SS. The slopes of linear fitted lines between calculated and observed NCCN are 0.708, 0.947, and 0.995 at SS of 0.1%, 0.2% and 0.4% respectively. Moreover, the stand deviation (SD) of calculated NCCN increased with the decreasing of SS. A case study of CCN closure analyses indicated that the calculated error of NCCN could reach up to 34% at SS of 0.1% if aerosol composition were not included, and the calculated error decreased with the raising of SS. It is decreased to 9% at SS of 0.2%, and further decreased to 4% at SS of 0.4%.

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